Canonical Allele Identifier: PA187969
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 184146
ClinVar RCV Id: RCV000163312 RCV000226413 RCV000454468 RCV001095934 RCV001083551 RCV001269363 RCV003153438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Met164Leu
CA016373
NM_003001.5:c.490A>T
CA343457937
NM_003001.5:c.490A>C