Canonical Allele Identifier: PA2825559276
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1189793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro188Ser
CA10558598
NM_001110792.2:c.562C>T