Canonical Allele Identifier: PA2829565088
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 548706
ClinVar RCV Id: RCV000662350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg190His
CA415173401
NM_004992.4:c.569G>A