Canonical Allele Identifier: PA2828325705
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ser308Asn
CA170203
NM_001369391.2:c.923G>A