Canonical Allele Identifier: PA2828327139
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Val207Ile
CA170394
NM_001369393.2:c.619G>A