Canonical Allele Identifier: PA2828325217
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1604076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Pro106Ser
CA415173156
NM_001369391.2:c.316C>T