Canonical Allele Identifier: PA2826942550
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_001298125.1:p.Arg311Ser
CA351005313
NM_001311196.2:c.933G>C
CA351005314
NM_001311196.2:c.933G>T