Allele Registry

Canonical Allele Identifier: PA915993741

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001376

ClinVar Variation:

1313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167561.1:p.Tyr487_Ala488delinsThr	CA354211 NM_001174090.2:c.1459_1462delinsA