Canonical Allele Identifier: PA2826955979
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro229Ser
CA121715
NM_001316337.2:c.685C>T