Canonical Allele Identifier: PA2826942305
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2164221
ClinVar RCV Id: RCV003082044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Asn239Ser
CA2168320
NM_001311195.2:c.716A>G