Canonical Allele Identifier: PA2825377997
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 161387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Ala3Val
CA011497
NM_001035513.2:c.8C>T