Canonical Allele Identifier: PA099149
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg167Trp
CA170308
NM_004992.4:c.499C>T