Canonical Allele Identifier: PA2826558543
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1430208
ClinVar RCV Id: RCV001967449 RCV004041936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Tyr105Phe
CA071391
NM_001276504.2:c.314A>T