Canonical Allele Identifier: PA2580129661
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2164221
ClinVar RCV Id: RCV003082044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Asn433Ser
CA2168320
NM_000751.2:c.1298A>G