Canonical Allele Identifier: PA658832418
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 547103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg145Ser
CA415175306
NM_001110792.2:c.433C>A