Canonical Allele Identifier: PA2580104165
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2156895
ClinVar RCV Id: RCV003075700 RCV003079449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.His647Tyr
CA361709462
NM_000112.4:c.1939C>T