Canonical Allele Identifier: PA645441180
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Lys125Asn
CA10582873
NM_003002.4:c.375G>T
CA382619055
NM_003002.4:c.375G>C