Allele Registry

Canonical Allele Identifier: PA2828704851

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000408624

ClinVar Variation:

369679

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Phe293Ser	CA10654763 NM_001377273.1:c.878T>C