Canonical Allele Identifier: PA297728
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_001120983.2:p.Ala367Val
CA004066
NM_001127511.3:c.1100C>T