Canonical Allele Identifier: PA2826558244
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_001263432.1:p.Leu63Phe
CA382618817
NM_001276503.2:c.189A>C
CA382618819
NM_001276503.2:c.189A>T