Canonical Allele Identifier: PA2829564851
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 560190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser70Pro
CA415177504
NM_004992.4:c.208T>C