Canonical Allele Identifier: PA2573065352
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301233
ClinVar RCV Id: RCV001733302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys212Thr
CA415173143
NM_001110792.2:c.635A>C