Canonical Allele Identifier: PA294712
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg202Cys
CA294710
NM_001110792.2:c.604C>T