Canonical Allele Identifier: PA2828328295
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro387Ser
CA170251
NM_001369394.2:c.1159C>T