Canonical Allele Identifier: PA270339
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143529
ClinVar RCV Id: RCV000133061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Trp116Arg
CA270337
NM_001110792.2:c.346T>C
CA415176872
NM_001110792.2:c.346T>A