Canonical Allele Identifier: PA2826955952
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg213Cys
CA212529
NM_001316337.2:c.637C>T