Canonical Allele Identifier: PA2828327269
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro268Ser
CA415168076
NM_001369393.2:c.802C>T