Canonical Allele Identifier: PA2826558812
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 955758
ClinVar RCV Id: RCV002241347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Leu75Phe
CA382617265
NM_001276506.2:c.225G>T
CA382617266
NM_001276506.2:c.225G>C