Canonical Allele Identifier: PA270314
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143515
ClinVar RCV Id: RCV000133046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro105Ser
CA270313
NM_001110792.2:c.313C>T