Canonical Allele Identifier: PA2825559227
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3024298
ClinVar RCV Id: RCV003883344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu150Phe
CA415175141
NM_001110792.2:c.450G>T
CA415175143
NM_001110792.2:c.450G>C