Canonical Allele Identifier: PA274841
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 192293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro229Ser
CA274839
NM_001110792.2:c.685C>T