Canonical Allele Identifier: PA2826956315
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009081
ClinVar RCV Id: RCV001306521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala353Val
CA10558438
NM_001316337.2:c.1058C>T