Canonical Allele Identifier: PA2828325890
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 835471
ClinVar RCV Id: RCV001036360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Leu15Phe
CA415176801
NM_001369392.2:c.43C>T