Allele Registry

Canonical Allele Identifier: PA156652

Gene: ALK HGNC NCBI

ClinVar RCV:

RCV000119982

RCV000731883

RCV001087719

RCV002257416

ClinVar Variation:

133478

HGVS (amino-acid)	Matching Registered Transcripts
NP_004295.2:p.Ala1396Thr	CA156650 NM_004304.5:c.4186G>A