Allele Registry

Canonical Allele Identifier: PA114923

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001382

ClinVar Variation:

1319

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Ser197Pro	CA114922 NM_001174089.2:c.589T>C