Canonical Allele Identifier: PA1139739130
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 850828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Asp281His
CA1593697
NM_001353765.2:c.841G>C