Allele Registry

Canonical Allele Identifier: PA260098

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029191

ClinVar Variation:

35536

HGVS (amino-acid)	Matching Registered Transcripts
NP_064693.2:p.His60Tyr	CA260095 NM_020297.3:c.178C>T