Canonical Allele Identifier: PA2826942171
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_001298124.1:p.Asn4Asp
CA350997459
NM_001311195.2:c.10A>G