Canonical Allele Identifier: PA916036111
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 65671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Phe177Val
CA345003
NM_001353765.2:c.529T>G