Canonical Allele Identifier: PA2828326748
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 393492
ClinVar RCV Id: RCV000445577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Thr12Pro
CA16609354
NM_001369393.2:c.34A>C