Allele Registry

Canonical Allele Identifier: PA2573074309

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000171207

ClinVar Variation:

191032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.His885Tyr	CA235865 NM_001377274.1:c.2653C>T