Canonical Allele Identifier: PA891866458
Gene: DCHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161708
ClinVar RCV Id: RCV000149244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345164.1:p.Gly1459Arg
CA174637
NM_001358235.2:c.4375G>A
CA358506108
NM_001358235.2:c.4375G>C