Canonical Allele Identifier: PA2826942560
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2164221
ClinVar RCV Id: RCV003082044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Asn332Ser
CA2168320
NM_001311196.2:c.995A>G