Canonical Allele Identifier: PA2826956361
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Thr386Met
CA170248
NM_001316337.2:c.1157C>T