Canonical Allele Identifier: PA2828327145
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro209Ser
CA270567
NM_001369393.2:c.625C>T