Canonical Allele Identifier: PA1139720740
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 844656
ClinVar RCV Id: RCV001047565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.His976Tyr
CA346468104
NM_004304.5:c.2926C>T