Canonical Allele Identifier: PA2828325178
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 493552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ser85Cys
CA10558596
NM_001369391.2:c.254C>G