Canonical Allele Identifier: PA2826107771
Gene: SLC4A11 HGNC NCBI

Linked Data

ClinVar Variation Id: 338232
ClinVar RCV Id: RCV000405940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167560.1:p.Ile852Val
CA10649519
NM_001174089.2:c.2554A>G