Canonical Allele Identifier: PA2826956133
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro291Leu
CA199482
NM_001316337.2:c.872C>T