Canonical Allele Identifier: PA2826942311
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 953201
ClinVar RCV Id: RCV001225459 RCV002227511 RCV003414021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Ile251Thr
CA2168324
NM_001311195.2:c.752T>C