Canonical Allele Identifier: PA2580145041
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2430069
ClinVar RCV Id: RCV003128034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg20Ser
CA415300864
NM_001110792.2:c.60A>T
CA415300867
NM_001110792.2:c.60A>C