Canonical Allele Identifier: PA2825377673
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 161387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Ala3Val
CA011497
NM_001035512.2:c.8C>T