Canonical Allele Identifier: PA2829069098
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Ala64Pro
CA270538
NM_001386138.1:c.190G>C