Canonical Allele Identifier: PA094095
Gene: SLC4A11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1306
ClinVar RCV Id: RCV000001369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114423.1:p.Gly464Asp
CA250437
NM_032034.4:c.1391G>A