Canonical Allele Identifier: PA2829564893
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 560189
ClinVar RCV Id: RCV000678234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser80Cys
CA415177339
NM_004992.4:c.239C>G