Canonical Allele Identifier: PA2828325839
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ser384Thr
CA170245
NM_001369391.2:c.1151G>C