Canonical Allele Identifier: PA916047809
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 493552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ser85Cys
CA10558596
NM_001369394.2:c.254C>G