Canonical Allele Identifier: PA2828325896
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143538
ClinVar RCV Id: RCV000133071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Arg18Gly
CA270357
NM_001369392.2:c.52A>G