Canonical Allele Identifier: PA2573078751
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Lys81Arg
CA170406
NM_001386139.1:c.242A>G