Canonical Allele Identifier: PA2828327790
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Leu235Val
CA270593
NM_001369394.2:c.703C>G