Canonical Allele Identifier: PA2828325780
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala346Ser
CA222801
NM_001369391.2:c.1036G>T