Canonical Allele Identifier: PA916047803
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro80Ala
CA270458
NM_001369394.2:c.238C>G