Canonical Allele Identifier: PA099522
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr158Ala
CA270438
NM_004992.4:c.472A>G