Canonical Allele Identifier: PA170250
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr491Met
CA170248
NM_001110792.2:c.1472C>T