Canonical Allele Identifier: PA2826955796
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014197
ClinVar RCV Id: RCV001312900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly138Trp
CA415172510
NM_001316337.2:c.412G>T