Canonical Allele Identifier: PA093963
Gene: SLC4A11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1314
ClinVar RCV Id: RCV000001377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114423.1:p.Arg488Lys
CA114916
NM_032034.4:c.1463G>A