Canonical Allele Identifier: PA2828325872
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143524
ClinVar RCV Id: RCV000133056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro8Ser
CA270328
NM_001369392.2:c.22C>T