Canonical Allele Identifier: PA2826558249
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2562396
ClinVar RCV Id: RCV003310456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Met66Ile
CA382618857
NM_001276503.2:c.198G>A
CA382618858
NM_001276503.2:c.198G>C
CA382618859
NM_001276503.2:c.198G>T