Canonical Allele Identifier: PA232970
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143581
ClinVar RCV Id: RCV000133119 RCV000170275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Phe155Cys
CA232969
NM_004992.4:c.464T>G