Canonical Allele Identifier: PA2828327430
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro306Ser
CA206184
NM_001369393.2:c.916C>T