Allele Registry

Canonical Allele Identifier: PA2828706271

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000426029

ClinVar Variation:

384013

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Ile1180Met	CA16607190 NM_001377274.1:c.3540T>G