Canonical Allele Identifier: PA2826955746
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala109Val
CA294713
NM_001316337.2:c.326C>T