Canonical Allele Identifier: PA2828326948
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1604076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro106Ser
CA415173156
NM_001369393.2:c.316C>T