Canonical Allele Identifier: PA2828325483
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Leu243Val
CA294661
NM_001369391.2:c.727C>G