Canonical Allele Identifier: PA2828325864
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143517
ClinVar RCV Id: RCV000133048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Asp4Tyr
CA270316
NM_001369392.2:c.10G>T