Canonical Allele Identifier: PA199326
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg309Trp
CA199325
NM_004992.4:c.925C>T