Canonical Allele Identifier: PA2828325427
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Lys211Arg
CA170406
NM_001369391.2:c.632A>G