Canonical Allele Identifier: PA2828326128
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro132Arg
CA270500
NM_001369392.2:c.395C>G