Canonical Allele Identifier: PA2826955631
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2673270
ClinVar RCV Id: RCV003457630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp58Val
CA415174729
NM_001316337.2:c.173A>T