Allele Registry

Canonical Allele Identifier: PA105606

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029189

RCV000809546

RCV001249678

RCV001699182

RCV002321487

ClinVar Variation:

35534

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg1116Cys	CA260087 NM_005691.3:c.3346C>T