Canonical Allele Identifier: PA916003559
Gene: SLC4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64516
ClinVar RCV Id: RCV000054703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186622.1:p.Pro9Leu
CA216321
NM_001199693.1:c.26C>T