Canonical Allele Identifier: PA2828325165
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Pro80Thr
CA415173958
NM_001369391.2:c.238C>A