Canonical Allele Identifier: PA2829068833
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro179Leu
CA199300
NM_001386137.1:c.536C>T