Canonical Allele Identifier: PA2828325657
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Pro295Ser
CA274535
NM_001369391.2:c.883C>T