Canonical Allele Identifier: PA294717
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156669
ClinVar RCV Id: RCV000726052 RCV000718449 RCV002265623 RCV002472364 RCV002514781 RCV004532634
ClinVar Variation Id: 2845786
ClinVar RCV Id: RCV003640178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly231Arg
CA294716
NM_004992.4:c.691G>A
CA415172511
NM_004992.4:c.691G>C