Canonical Allele Identifier: PA2829068951
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Glu250Asp
CA10558429
NM_001386137.1:c.750G>C
CA415163273
NM_001386137.1:c.750G>T