Canonical Allele Identifier: PA2829412496
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3073872
ClinVar RCV Id: RCV004012414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Leu77Gln
CA382617275
NM_003002.4:c.230T>A