Canonical Allele Identifier: PA2826955605
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3024298
ClinVar RCV Id: RCV003883344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Leu45Phe
CA415175141
NM_001316337.2:c.135G>T
CA415175143
NM_001316337.2:c.135G>C