Allele Registry

Canonical Allele Identifier: PA2829622331

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000426029

ClinVar Variation:

384013

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Ile1469Met	CA16607190 NM_005691.3:c.4407T>G