Canonical Allele Identifier: PA2829565019
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804127
ClinVar RCV Id: RCV000991002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Asp156Tyr
CA415174595
NM_004992.4:c.466G>T