Canonical Allele Identifier: PA2826955938
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ile210Met
CA170403
NM_001316337.2:c.630C>G