Canonical Allele Identifier: PA2828326310
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Arg216Trp
CA199325
NM_001369392.2:c.646C>T