Canonical Allele Identifier: PA2828326975
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143642
ClinVar RCV Id: RCV000133182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Lys117Ile
CA270490
NM_001369393.2:c.350A>T