Canonical Allele Identifier: PA294711
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg190Cys
CA294710
NM_004992.4:c.568C>T