Canonical Allele Identifier: PA2828328029
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468919
ClinVar RCV Id: RCV001972893 RCV002280200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Val119Asp
CA415172922
NM_001369394.2:c.356T>A