Canonical Allele Identifier: PA2826649019
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 2664894
ClinVar RCV Id: RCV003447868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269460.1:p.Tyr172His
CA408977551
NM_001282531.3:c.514T>C