Canonical Allele Identifier: PA2828327010
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014197
ClinVar RCV Id: RCV001312900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Gly138Trp
CA415172510
NM_001369393.2:c.412G>T