Canonical Allele Identifier: PA2828325983
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro59Ala
CA121717
NM_001369392.2:c.175C>G