Canonical Allele Identifier: PA232992
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro225Thr
CA232991
NM_004992.4:c.673C>A