Canonical Allele Identifier: PA2829068555
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Lys81Arg
CA170406
NM_001386137.1:c.242A>G