Canonical Allele Identifier: PA2828326766
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431705
ClinVar RCV Id: RCV000655939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Gly21_Ser23del
CA658799902
NM_001369393.2:c.62_70del