Canonical Allele Identifier: PA2826942559
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 935357
ClinVar RCV Id: RCV001203928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Glu329Asp
CA351005562
NM_001311196.2:c.987A>C
CA351005564
NM_001311196.2:c.987A>T