Allele Registry

Canonical Allele Identifier: PA094258

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001384

RCV002281686

ClinVar Variation:

1321

HGVS (amino-acid)	Matching Registered Transcripts
NP_114423.1:p.Thr754Met	CA114927 NM_032034.4:c.2261C>T