Canonical Allele Identifier: PA2573078771
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro99Ala
CA274540
NM_001386139.1:c.295C>G