Canonical Allele Identifier: PA2826955560
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576682
ClinVar RCV Id: RCV003322987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Tyr27Cys
CA415176540
NM_001316337.2:c.80A>G