Canonical Allele Identifier: PA2828326881
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Arg74Trp
CA170308
NM_001369393.2:c.220C>T