Canonical Allele Identifier: PA2829936505
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685629
ClinVar RCV Id: RCV002249356
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Glu1201Asp
CA388894060
NM_020920.4:c.3603G>T
CA388894061
NM_020920.4:c.3603G>C