Canonical Allele Identifier: PA2829069547
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro257Ser
CA170251
NM_001386138.1:c.769C>T