Canonical Allele Identifier: PA2826942562
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 835938
ClinVar RCV Id: RCV001036943 RCV004031012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Asp339Val
CA2168322
NM_001311196.2:c.1016A>T