Canonical Allele Identifier: PA916036190
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 470871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Ser380Phe
CA346462550
NM_001353765.2:c.1139C>T