Canonical Allele Identifier: PA2828325985
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Phe62Cys
CA232969
NM_001369392.2:c.185T>G