Canonical Allele Identifier: PA198823
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11835
ClinVar RCV Id: RCV000012608 RCV000498874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu112Val
CA198822
NM_001110792.2:c.334C>G