Canonical Allele Identifier: PA2826955599
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys42Glu
CA270401
NM_001316337.2:c.124A>G