Canonical Allele Identifier: PA916006150
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412500
ClinVar RCV Id: RCV002230659 RCV002323760 RCV003476140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Val71Ile
CA16613228
NM_001276504.2:c.211G>A