Canonical Allele Identifier: PA270391
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143560
ClinVar RCV Id: RCV000133093 RCV001565841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg133Leu
CA270390
NM_004992.4:c.398G>T