Canonical Allele Identifier: PA658825258
Gene: CHD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 520977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005273.1:p.Arg985Trp
CA397940726
NM_001005273.3:c.2953C>T