Canonical Allele Identifier: PA2826401513
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1304198
ClinVar RCV Id: RCV001751965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Arg397Ser
CA351005313
NM_001256657.2:c.1191G>C
CA351005314
NM_001256657.2:c.1191G>T