Canonical Allele Identifier: PA2580145038
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2032447
ClinVar RCV Id: RCV002876994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly13Arg
CA415301203
NM_001110792.2:c.37G>C
CA415301206
NM_001110792.2:c.37G>A