Canonical Allele Identifier: PA916006126
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412507
ClinVar RCV Id: RCV001764454 RCV002525626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gln84His
CA16613234
NM_001276503.2:c.252G>C
CA382619208
NM_001276503.2:c.252G>T