Canonical Allele Identifier: PA2826955600
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2019735
ClinVar RCV Id: RCV002852039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys42Asn
CA415175214
NM_001316337.2:c.126A>T
CA415175219
NM_001316337.2:c.126A>C