Canonical Allele Identifier: PA2826955882
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala186Val
CA270535
NM_001316337.2:c.557C>T