Canonical Allele Identifier: PA2829068964
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Val258Met
CA208886
NM_001386137.1:c.772G>A