Canonical Allele Identifier: PA094364
Gene: SLC4A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17760
ClinVar RCV Id: RCV000019337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000333.1:p.Gly771Asp
CA127382
NM_000342.4:c.2312G>A