Canonical Allele Identifier: PA263249
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 56012
ClinVar RCV Id: RCV000049421 RCV001388086 RCV003474627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Ala386Val
CA263247
NM_000112.4:c.1157C>T