Canonical Allele Identifier: PA2829685984
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 3157834
ClinVar RCV Id: RCV004450155
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009032.2:p.Gly260Asp
CA5314673
NM_007101.3:c.779G>A