Canonical Allele Identifier: PA170425
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Lys331Arg
CA170424
NM_004992.4:c.992A>G