Canonical Allele Identifier: PA2829412582
Gene: SDHD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.His102Pro
CA382617414
NM_003002.4:c.305A>C