Canonical Allele Identifier: PA2828325841
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg385Gln
CA199452
NM_001369391.2:c.1154G>A