Canonical Allele Identifier: PA099096
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala140Val
CA121703
NM_004992.4:c.419C>T