Canonical Allele Identifier: PA156649
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133477
ClinVar RCV Id: RCV000119981 RCV000472979 RCV001356607 RCV002257415 RCV003935135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Pro1599His
CA156647
NM_004304.5:c.4796C>A