Canonical Allele Identifier: PA2828325469
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Leu235Val
CA270593
NM_001369391.2:c.703C>G