Canonical Allele Identifier: PA2828328034
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro132Thr
CA232991
NM_001369394.2:c.394C>A