Allele Registry

Canonical Allele Identifier: PA102994

Gene: BAAT HGNC NCBI

ClinVar RCV:

RCV000007112

ClinVar Variation:

6720

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121082.1:p.Met76Val	CA118444 NM_001127610.2:c.226A>G