Canonical Allele Identifier: PA2829068981
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro2Arg
CA270500
NM_001386138.1:c.5C>G