Canonical Allele Identifier: PA2825377520
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 2447630
ClinVar RCV Id: RCV003165339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030588.1:p.Pro54Leu
CA343361290
NM_001035511.2:c.161C>T