Canonical Allele Identifier: PA2826246551
Gene: SLC4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64510
ClinVar RCV Id: RCV000054697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186623.1:p.Ala1033Val
CA216309
NM_001199694.2:c.3098C>T