Canonical Allele Identifier: PA2829069172
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro99Ser
CA121715
NM_001386138.1:c.295C>T