Canonical Allele Identifier: PA2826955735
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1604076
ClinVar RCV Id: RCV002149391 RCV004531417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro106Ser
CA415173156
NM_001316337.2:c.316C>T