Canonical Allele Identifier: PA2826955562
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 995700
ClinVar RCV Id: RCV001810713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp28Glu
CA415176488
NM_001316337.2:c.84T>A
CA415176490
NM_001316337.2:c.84T>G