Canonical Allele Identifier: PA916047813
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143618
ClinVar RCV Id: RCV000133158 RCV003990991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly90Arg
CA170325
NM_001369394.2:c.268G>C
CA415173745
NM_001369394.2:c.268G>A