Canonical Allele Identifier: PA2741936950
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2591889
ClinVar RCV Id: RCV004341495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009032.2:p.Glu299Asp
CA5314622
NM_007101.3:c.897G>C
CA375426015
NM_007101.3:c.897G>T