Canonical Allele Identifier: PA2828326979
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Val119Asp
CA415172922
NM_001369393.2:c.356T>A