Allele Registry

Canonical Allele Identifier: PA2573074321

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000487267

ClinVar Variation:

420903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Ser924Ala	CA16619502 NM_001377274.1:c.2770T>G