Canonical Allele Identifier: PA2828325011
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Gly10Asp
CA270334
NM_001369391.2:c.29G>A