Canonical Allele Identifier: PA2826246449
Gene: SLC4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64508
ClinVar RCV Id: RCV000054695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186622.1:p.Ala739Ser
CA216305
NM_001199693.1:c.2215G>T