Canonical Allele Identifier: PA2828325133
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Thr65Met
CA211252
NM_001369391.2:c.194C>T