Canonical Allele Identifier: PA2826955629
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asp58Gly
CA270421
NM_001316337.2:c.173A>G