Allele Registry

Canonical Allele Identifier: PA105679

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029191

ClinVar Variation:

35536

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.His60Tyr	CA260095 NM_005691.3:c.178C>T