Canonical Allele Identifier: PA2826558396
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 955758
ClinVar RCV Id: RCV002241347
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Leu36Phe
CA382617265
NM_001276504.2:c.108G>T
CA382617266
NM_001276504.2:c.108G>C