Canonical Allele Identifier: PA2827399935
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 521542
ClinVar RCV Id: RCV000622881 RCV001265428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334440.1:p.Gln67His
CA408981381
NM_001347511.2:c.201G>T
CA408981383
NM_001347511.2:c.201G>C