Canonical Allele Identifier: PA2829068728
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro158Ser
CA10558497
NM_001386137.1:c.472C>T