Canonical Allele Identifier: PA2827737338
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 217849
ClinVar RCV Id: RCV000201883 RCV000421904
ClinVar Variation Id: 217851
ClinVar RCV Id: RCV000201882 RCV000418576 RCV000426846 RCV000435780 RCV000444781
ClinVar Variation Id: 217852
ClinVar RCV Id: RCV000201904 RCV000442440 RCV000427324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Phe106Leu
CA277829
NM_001353765.2:c.316T>C
CA279586
NM_001353765.2:c.318C>A
CA279616
NM_001353765.2:c.318C>G