Allele Registry

Canonical Allele Identifier: PA2829120857

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373542.1:p.Leu412Pro	CA175088 NM_001386613.1:c.1235T>C