Canonical Allele Identifier: PA645503011
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407056
ClinVar RCV Id: RCV000472364 RCV001016164 RCV001770320 RCV003476038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Ser88Leu
CA047197
NM_003001.5:c.263C>T