Canonical Allele Identifier: PA2573078756
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Lys82Arg
CA270586
NM_001386139.1:c.245A>G