Allele Registry

Canonical Allele Identifier: PA2829915855

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV001901407

ClinVar Variation:

1403970

HGVS (amino-acid)	Matching Registered Transcripts
NP_064693.2:p.Arg1154Pro	CA6481113 NM_020297.3:c.3461G>C