Canonical Allele Identifier: PA297729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181784
ClinVar RCV Id: RCV000159529 RCV002516407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala385Val
CA004066
NM_000038.6:c.1154C>T