Canonical Allele Identifier: PA256096
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala2Val
CA256095
NM_001110792.2:c.5C>T