Allele Registry

Canonical Allele Identifier: PA114928

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001384

RCV002281686

ClinVar Variation:

1321

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Thr738Met	CA114927 NM_001174089.2:c.2213C>T