Canonical Allele Identifier: PA2828325043
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098273
ClinVar RCV Id: RCV001420143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Asp28Val
CA415176492
NM_001369391.2:c.83A>T