Canonical Allele Identifier: PA2828325868
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Leu7Val
CA198822
NM_001369392.2:c.19C>G