Canonical Allele Identifier: PA294721
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156670
ClinVar RCV Id: RCV000723954 RCV001079662 RCV002362777 RCV002472365 RCV004544329
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala246Gly
CA294719
NM_001110792.2:c.737C>G