Allele Registry

Canonical Allele Identifier: PA2828109006

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001376

ClinVar Variation:

1313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350674.1:p.Tyr406_Ala407delinsThr	CA354211 NM_001363745.1:c.1216_1219delinsA