Canonical Allele Identifier: PA645400907
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 393492
ClinVar RCV Id: RCV000445577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr117Pro
CA16609354
NM_001110792.2:c.349A>C