Canonical Allele Identifier: PA2828326744
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143529
ClinVar RCV Id: RCV000133061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Trp11Arg
CA270337
NM_001369393.2:c.31T>C
CA415176872
NM_001369393.2:c.31T>A