Canonical Allele Identifier: PA2828325226
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala109Val
CA294713
NM_001369391.2:c.326C>T