Canonical Allele Identifier: PA2826956122
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro288Ser
CA10558497
NM_001316337.2:c.862C>T