Canonical Allele Identifier: PA2741809427
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945503
ClinVar RCV Id: RCV003803597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Gly242Val
CA361706130
NM_000112.4:c.725G>T