Canonical Allele Identifier: PA2826942520
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 847481
ClinVar RCV Id: RCV001051039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Pro268Arg
CA351005042
NM_001311196.2:c.803C>G