Canonical Allele Identifier: PA170407
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Lys304Arg
CA170406
NM_004992.4:c.911A>G