Canonical Allele Identifier: PA2826955698
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446116
ClinVar RCV Id: RCV003156470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro86Leu
CA415173812
NM_001316337.2:c.257C>T