Allele Registry

Canonical Allele Identifier: PA250443

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001372

RCV001682704

ClinVar Variation:

1309

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Arg853Cys	CA250442 NM_001174089.2:c.2557C>T