Canonical Allele Identifier: PA2826955785
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016198
ClinVar RCV Id: RCV003876349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gln134His
CA10558567
NM_001316337.2:c.402A>C
CA10558569
NM_001316337.2:c.402A>T