Allele Registry

Canonical Allele Identifier: PA2829621872

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000487267

ClinVar Variation:

420903

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Ser1213Ala	CA16619502 NM_005691.3:c.3637T>G