Canonical Allele Identifier: PA658666523
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465238
ClinVar RCV Id: RCV002526127 RCV003999154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly138Val
CA382619290
NM_003002.4:c.413G>T