Canonical Allele Identifier: PA2828326288
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Ile210Met
CA170403
NM_001369392.2:c.630C>G