Canonical Allele Identifier: PA2826955561
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098273
ClinVar RCV Id: RCV001420143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp28Val
CA415176492
NM_001316337.2:c.83A>T