Canonical Allele Identifier: PA156658
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133480
ClinVar RCV Id: RCV000119984 RCV000233768 RCV001575009 RCV002255291 RCV003905136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Arg311His
CA156656
NM_004304.5:c.932G>A