Allele Registry

Canonical Allele Identifier: PA114925

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001383

ClinVar Variation:

1320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Gly693Glu	CA114924 NM_001174089.2:c.2078G>A