Canonical Allele Identifier: PA658679292
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 470772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Ala586Thr
CA1594541
NM_004304.5:c.1756G>A