Allele Registry

Canonical Allele Identifier: PA2826107505

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001376

ClinVar Variation:

1313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Tyr444_Ala445delinsThr	CA354211 NM_001174089.2:c.1330_1333delinsA