Canonical Allele Identifier: PA2829522438
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 1732850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Phe1193Leu
CA346473074
NM_004304.5:c.3579C>G
CA346473075
NM_004304.5:c.3579C>A
CA346473081
NM_004304.5:c.3577T>C