Canonical Allele Identifier: PA2827738145
Gene: CLHC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 183280
ClinVar RCV Id: RCV000162101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340709.1:p.Arg316Gln
CA186043
NM_001353780.2:c.947G>A