Canonical Allele Identifier: PA2573078769
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro99Leu
CA270591
NM_001386139.1:c.296C>T