Canonical Allele Identifier: PA2828326843
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Asp58Gly
CA270421
NM_001369393.2:c.173A>G