Canonical Allele Identifier: PA2825559183
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg103Gln
CA10558642
NM_001110792.2:c.308G>A