Canonical Allele Identifier: PA2828325018
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg13Gly
CA270345
NM_001369391.2:c.37C>G