Canonical Allele Identifier: PA916036130
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 217858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Tyr210Ser
CA279600
NM_001353765.2:c.629A>C