Allele Registry

Canonical Allele Identifier: PA114926

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001383

ClinVar Variation:

1320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167561.1:p.Gly736Glu	CA114924 NM_001174090.2:c.2207G>A