Canonical Allele Identifier: PA2828325801
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala354Thr
CA170236
NM_001369391.2:c.1060G>A