Canonical Allele Identifier: PA2828326058
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2117601
ClinVar RCV Id: RCV003027825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Gly92Cys
CA415173667
NM_001369392.2:c.274G>T