Canonical Allele Identifier: PA2828327599
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly10Asp
CA270334
NM_001369394.2:c.29G>A