Canonical Allele Identifier: PA2828325434
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg213Leu
CA233016
NM_001369391.2:c.638G>T