Canonical Allele Identifier: PA156619
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133467
ClinVar RCV Id: RCV000119971 RCV000475908 RCV002257413 RCV002266923 RCV003952583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Pro1027Leu
CA156617
NM_004304.5:c.3080C>T