Canonical Allele Identifier: PA2829069062
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Arg45Trp
CA233007
NM_001386138.1:c.133C>T