Canonical Allele Identifier: PA2828326173
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Arg157Cys
CA205183
NM_001369392.2:c.469C>T