Canonical Allele Identifier: PA916047802
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro80Thr
CA415173958
NM_001369394.2:c.238C>A