Canonical Allele Identifier: PA2580129662
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1944674
ClinVar RCV Id: RCV002639897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Ala442Val
CA351005708
NM_000751.2:c.1325C>T