Canonical Allele Identifier: PA2828325857
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003411
ClinVar RCV Id: RCV001299959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Val392Leu
CA10558426
NM_001369391.2:c.1174G>C