Canonical Allele Identifier: PA170360
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser241Leu
CA170358
NM_001110792.2:c.722C>T