Canonical Allele Identifier: PA2828326750
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Arg13Trp
CA256089
NM_001369393.2:c.37C>T