Canonical Allele Identifier: PA658666453
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 466190
ClinVar RCV Id: RCV000542114 RCV001141061 RCV000762329
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Asn456Ser
CA2168330
NM_000751.2:c.1367A>G