Canonical Allele Identifier: PA2828326758
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406613
ClinVar RCV Id: RCV001915903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Leu15Val
CA415176805
NM_001369393.2:c.43C>G