Canonical Allele Identifier: PA2828325073
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Arg40Leu
CA270390
NM_001369391.2:c.119G>T