Allele Registry

Canonical Allele Identifier: PA2825645898

Gene: BAAT HGNC NCBI

ClinVar RCV:

RCV000020464

ClinVar Variation:

21301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121082.1:p.Ile323Val	CA341872 NM_001127610.2:c.967A>G