Canonical Allele Identifier: PA272983
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 161387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Ala3Val
CA011497
NM_003001.5:c.8C>T