Canonical Allele Identifier: PA2580229883
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1745655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro79Ala
CA415173980
NM_001369394.2:c.235C>G