Canonical Allele Identifier: PA170205
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143435
ClinVar RCV Id: RCV000132961 RCV002055850 RCV003380461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser413Asn
CA170203
NM_001110792.2:c.1238G>A