Canonical Allele Identifier: PA279620
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 217854
ClinVar RCV Id: RCV000201906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Leu1240Val
CA279618
NM_004304.5:c.3718T>G