Canonical Allele Identifier: PA916036082
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 470837
ClinVar Variation Id: 569205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Met131Leu
CA346473043
NM_001353765.2:c.391A>T
CA346473045
NM_001353765.2:c.391A>C