Canonical Allele Identifier: PA2828326800
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Ala38Asp
CA270384
NM_001369393.2:c.113C>A