Allele Registry

Canonical Allele Identifier: PA105599

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000024627

ClinVar Variation:

31949

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Ala478Val	CA260070 NM_005691.3:c.1433C>T