Canonical Allele Identifier: PA170410
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr311Met
CA170409
NM_004992.4:c.932C>T