Canonical Allele Identifier: PA2828327674
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ala146Asp
CA415172315
NM_001369394.2:c.437C>A