Canonical Allele Identifier: PA2573227480
Gene: SDHD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ser32Leu
CA382616984
NM_003002.4:c.95C>T