Canonical Allele Identifier: PA2826955558
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432216
ClinVar RCV Id: RCV000498617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly25Ala
CA415176592
NM_001316337.2:c.74G>C