Allele Registry

Canonical Allele Identifier: PA2573074282

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000408624

ClinVar Variation:

369679

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Phe5Ser	CA10654763 NM_001377274.1:c.14T>C