Canonical Allele Identifier: PA2829565798
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1667533
ClinVar RCV Id: RCV002195782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Glu472Asp
CA415163310
NM_004992.4:c.1416G>C
CA415163315
NM_004992.4:c.1416G>T