Canonical Allele Identifier: PA2829069162
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Thr88Met
CA170409
NM_001386138.1:c.263C>T