Canonical Allele Identifier: PA2829068669
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429415
ClinVar RCV Id: RCV000493837 RCV001257760 RCV001312686 RCV003448314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro139Ser
CA415168068
NM_001386137.1:c.415C>T