Canonical Allele Identifier: PA2825559204
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576682
ClinVar RCV Id: RCV003322987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Tyr132Cys
CA415176540
NM_001110792.2:c.395A>G