Canonical Allele Identifier: PA2499234117
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1022451
ClinVar RCV Id: RCV001322361
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Glu94Gly
CA350997459
NM_000751.2:c.281A>G