Canonical Allele Identifier: PA2828325341
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg175Trp
CA233007
NM_001369391.2:c.523C>T