Canonical Allele Identifier: PA2828325243
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143642
ClinVar RCV Id: RCV000133182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Lys117Ile
CA270490
NM_001369391.2:c.350A>T