Canonical Allele Identifier: PA2826955680
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928877
ClinVar RCV Id: RCV001193434 RCV001344042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro79Thr
CA415173983
NM_001316337.2:c.235C>A