Canonical Allele Identifier: PA2573063715
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1302902
ClinVar RCV Id: RCV001756401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Asn443Ser
CA351005718
NM_000751.2:c.1328A>G