Canonical Allele Identifier: PA2826956221
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ser308Asn
CA170203
NM_001316337.2:c.923G>A