Canonical Allele Identifier: PA2828325283
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala141Gly
CA294719
NM_001369391.2:c.422C>G