Canonical Allele Identifier: PA2825378060
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407061
ClinVar RCV Id: RCV000461822 RCV002446798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Val29Phe
CA047220
NM_001035513.2:c.85G>T