Canonical Allele Identifier: PA169721
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 142904
ClinVar RCV Id: RCV000132372 RCV000534423 RCV002254682 RCV002483272 RCV003474790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Pro146Thr
CA016343
NM_003001.5:c.436C>A