Canonical Allele Identifier: PA2828327776
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg213Cys
CA212529
NM_001369394.2:c.637C>T