Canonical Allele Identifier: PA2828325879
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632618
ClinVar RCV Id: RCV004528687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Trp11Gly
CA415176868
NM_001369392.2:c.31T>G