Canonical Allele Identifier: PA2829069541
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Ser254Thr
CA170245
NM_001386138.1:c.761G>C