Canonical Allele Identifier: PA2826955656
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143596
ClinVar RCV Id: RCV000133135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly68Trp
CA270443
NM_001316337.2:c.202G>T