Canonical Allele Identifier: PA270573
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro314Arg
CA270572
NM_001110792.2:c.941C>G