Canonical Allele Identifier: PA1139738782
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 849292
ClinVar RCV Id: RCV001053220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Leu122Pro
CA346473090
NM_001353765.2:c.365T>C