Canonical Allele Identifier: PA2829068545
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro79Ser
CA270567
NM_001386137.1:c.235C>T