Canonical Allele Identifier: PA916047761
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys42Glu
CA270401
NM_001369394.2:c.124A>G