Canonical Allele Identifier: PA2828326325
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro229Ala
CA274540
NM_001369392.2:c.685C>G