Canonical Allele Identifier: PA156622
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133468
ClinVar RCV Id: RCV000119972 RCV000465205 RCV001018784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Ala1047Thr
CA156620
NM_004304.5:c.3139G>A