Canonical Allele Identifier: PA093477
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 376713
ClinVar RCV Id: RCV000422585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Met1166Arg
CA16603123
NM_004304.5:c.3497T>G