Canonical Allele Identifier: PA2829412616
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2567227
ClinVar RCV Id: RCV003278397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Thr112Ser
CA382618819
NM_003002.4:c.334A>T
CA382618822
NM_003002.4:c.335C>G