Canonical Allele Identifier: PA2828326957
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Ala108Val
CA211932
NM_001369393.2:c.323C>T