Canonical Allele Identifier: PA916036108
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 217857
ClinVar RCV Id: RCV000201908
ClinVar Variation Id: 375885
ClinVar RCV Id: RCV000434421
ClinVar Variation Id: 376712
ClinVar RCV Id: RCV000432633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Phe177Leu
CA279621
NM_001353765.2:c.531C>A
CA16602368
NM_001353765.2:c.531C>G
CA16603122
NM_001353765.2:c.529T>C