Canonical Allele Identifier: PA2828326931
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 566728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Arg95Trp
CA10558590
NM_001369393.2:c.283C>T