Canonical Allele Identifier: PA2828325696
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Pro306Ser
CA206184
NM_001369391.2:c.916C>T