Canonical Allele Identifier: PA2826955770
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 807854
ClinVar RCV Id: RCV000996058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys122Gln
CA415172871
NM_001316337.2:c.364A>C