Canonical Allele Identifier: PA170301
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143575
ClinVar RCV Id: RCV000133111 RCV003990986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp159Asn
CA170299
NM_001110792.2:c.475G>A