Canonical Allele Identifier: PA2825559180
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 590069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg101Cys
CA10558644
NM_001110792.2:c.301C>T