Canonical Allele Identifier: PA645441115
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 420665
ClinVar RCV Id: RCV000479419 RCV000569878 RCV002525847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Asp92Val
CA16619272
NM_003002.4:c.275A>T