Canonical Allele Identifier: PA099399
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1324711
ClinVar RCV Id: RCV001782431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro101Thr
CA415176913
NM_004992.4:c.301C>A