Allele Registry

Canonical Allele Identifier: PA260094

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029190

ClinVar Variation:

35535

HGVS (amino-acid)	Matching Registered Transcripts
NP_064693.2:p.Ser1020Pro	CA260091 NM_020297.3:c.3058T>C