Canonical Allele Identifier: PA2828325871
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143527
ClinVar RCV Id: RCV000133059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro8Leu
CA270332
NM_001369392.2:c.23C>T