Canonical Allele Identifier: PA2826955516
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143517
ClinVar RCV Id: RCV000133048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp4Tyr
CA270316
NM_001316337.2:c.10G>T