Canonical Allele Identifier: PA2826955704
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala88Val
CA170322
NM_001316337.2:c.263C>T