Canonical Allele Identifier: PA2828109281
Gene: SLC4A11 HGNC NCBI

Linked Data

ClinVar Variation Id: 338232
ClinVar RCV Id: RCV000405940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350674.1:p.Ile814Val
CA10649519
NM_001363745.1:c.2440A>G