Canonical Allele Identifier: PA2828327216
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Leu243Val
CA294661
NM_001369393.2:c.727C>G