Canonical Allele Identifier: PA2826649333
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 434095
ClinVar RCV Id: RCV000499393 RCV000764249 RCV001545023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269460.1:p.Asp873Tyr
CA9908560
NM_001282531.3:c.2617G>T