Canonical Allele Identifier: PA916047765
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ala47Val
CA121703
NM_001369394.2:c.140C>T