Canonical Allele Identifier: PA916047750
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gln35Pro
CA270379
NM_001369394.2:c.104A>C