Canonical Allele Identifier: PA916036191
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 335689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Ala391Ser
CA1593586
NM_001353765.2:c.1171G>T