Allele Registry

Canonical Allele Identifier: PA2827737338

Gene: ALK HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000201882

RCV000201883

RCV000201904

RCV000418576

RCV000421904

RCV000426846

RCV000427324

RCV000435780

RCV000442440

RCV000444781

ClinVar Variation:

217849

217851

217852

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340694.1:p.Phe106Leu	CA277829 NM_001353765.2:c.316T>C CA279586 NM_001353765.2:c.318C>A CA279616 NM_001353765.2:c.318C>G