Canonical Allele Identifier: PA2826955706
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721248
ClinVar RCV Id: RCV002294928 RCV002510602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro89Ser
CA415173760
NM_001316337.2:c.265C>T