Canonical Allele Identifier: PA2828326067
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Arg97Cys
CA294710
NM_001369392.2:c.289C>T