Canonical Allele Identifier: PA2828327177
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Thr218Met
CA170409
NM_001369393.2:c.653C>T