Canonical Allele Identifier: PA2826955946
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys212Arg
CA270586
NM_001316337.2:c.635A>G