Canonical Allele Identifier: PA099227
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143517
ClinVar RCV Id: RCV000133048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Asp97Tyr
CA270316
NM_004992.4:c.289G>T