Canonical Allele Identifier: PA170279
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Lys82Arg
CA170278
NM_004992.4:c.245A>G