Canonical Allele Identifier: PA2829564895
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser80Phe
CA415177336
NM_004992.4:c.239C>T