Canonical Allele Identifier: PA2828325306
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg157Cys
CA205183
NM_001369391.2:c.469C>T