Canonical Allele Identifier: PA2825559197
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406613
ClinVar RCV Id: RCV001915903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu120Val
CA415176805
NM_001110792.2:c.358C>G