Canonical Allele Identifier: PA294714
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156668
ClinVar RCV Id: RCV000144811 RCV003227673 RCV002055866 RCV004532633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala202Val
CA294713
NM_004992.4:c.605C>T