Allele Registry

Canonical Allele Identifier: PA094218

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001382

ClinVar Variation:

1319

HGVS (amino-acid)	Matching Registered Transcripts
NP_114423.1:p.Ser213Pro	CA114922 NM_032034.4:c.637T>C