Canonical Allele Identifier: PA2826955590
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg40Leu
CA270390
NM_001316337.2:c.119G>T