Canonical Allele Identifier: PA170395
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Val300Ile
CA170394
NM_004992.4:c.898G>A