Canonical Allele Identifier: PA2829564950
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432216
ClinVar RCV Id: RCV000498617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly118Ala
CA415176592
NM_004992.4:c.353G>C