Canonical Allele Identifier: PA2825559196
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 835471
ClinVar RCV Id: RCV001036360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu120Phe
CA415176801
NM_001110792.2:c.358C>T