Allele Registry

Canonical Allele Identifier: PA156661

Gene: ALK HGNC NCBI

ClinVar RCV:

RCV000119985

RCV000463094

RCV003126501

ClinVar Variation:

133481

HGVS (amino-acid)	Matching Registered Transcripts
NP_004295.2:p.Phe270Leu	CA156659 NM_004304.5:c.808T>C CA44976851 NM_004304.5:c.810C>G CA346587099 NM_004304.5:c.810C>A