Canonical Allele Identifier: PA2826401531
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2440045
ClinVar RCV Id: RCV003144945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Met434Ile
CA351005805
NM_001256657.2:c.1302G>A
CA351005806
NM_001256657.2:c.1302G>C
CA351005807
NM_001256657.2:c.1302G>T