Canonical Allele Identifier: PA2499254411
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1189793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro83Ser
CA10558598
NM_001369394.2:c.247C>T