Canonical Allele Identifier: PA2580226723
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 1739722
ClinVar RCV Id: RCV002332059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340694.1:p.Pro374Ser
CA346462632
NM_001353765.2:c.1120C>T