Canonical Allele Identifier: PA2828326987
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 192293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro124Ser
CA274839
NM_001369393.2:c.370C>T