Canonical Allele Identifier: PA2826942314
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 466190
ClinVar RCV Id: RCV000542114 RCV001141061 RCV000762329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Asn262Ser
CA2168330
NM_001311195.2:c.785A>G