Canonical Allele Identifier: PA274629
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143585
ClinVar RCV Id: RCV000133123 RCV000170239 RCV001815200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Phe157Ile
CA274628
NM_004992.4:c.469T>A