Canonical Allele Identifier: PA2573078738
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Val77Ile
CA170394
NM_001386139.1:c.229G>A