Canonical Allele Identifier: PA2829069309
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Ala155Val
CA170175
NM_001386138.1:c.464C>T