Canonical Allele Identifier: PA2828325113
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Asp58Tyr
CA415174739
NM_001369391.2:c.172G>T