Canonical Allele Identifier: PA2829565489
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro381Ser
CA10558497
NM_004992.4:c.1141C>T