Canonical Allele Identifier: PA658679412
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 470837
ClinVar Variation Id: 569205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Met1199Leu
CA346473043
NM_004304.5:c.3595A>T
CA346473045
NM_004304.5:c.3595A>C