Canonical Allele Identifier: PA2826955699
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432900
ClinVar RCV Id: RCV000497938 RCV001070300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro86Ala
CA415173835
NM_001316337.2:c.256C>G