Canonical Allele Identifier: PA916047720
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro8Arg
CA274626
NM_001369394.2:c.23C>G