Canonical Allele Identifier: PA645396833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468
ClinVar RCV Id: RCV000220684 RCV002229315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala987Val
CA10578347
NM_001127511.3:c.2960C>T