Allele Registry

Canonical Allele Identifier: PA236326

Gene: BAAT HGNC NCBI

ClinVar RCV:

RCV000171425

RCV000333195

RCV003984825

ClinVar Variation:

191236

HGVS (amino-acid)	Matching Registered Transcripts
NP_001692.1:p.Thr254Met	CA236325 NM_001701.4:c.761C>T