Canonical Allele Identifier: PA2826942309
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1302902
ClinVar RCV Id: RCV001756401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Asn249Ser
CA351005718
NM_001311195.2:c.746A>G