Canonical Allele Identifier: PA645502974
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407053
ClinVar RCV Id: RCV000472430 RCV001027045 RCV002481414 RCV003233639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Ala3Ser
CA048618
NM_003001.5:c.7G>T