Canonical Allele Identifier: PA2825559246
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066414
ClinVar RCV Id: RCV003991418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro164Leu
CA415174704
NM_001110792.2:c.491C>T