Canonical Allele Identifier: PA2825559193
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632618
ClinVar RCV Id: RCV004528687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Trp116Gly
CA415176868
NM_001110792.2:c.346T>G