Canonical Allele Identifier: PA2829565800
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Glu473Asp
CA10558429
NM_004992.4:c.1419G>C
CA415163273
NM_004992.4:c.1419G>T