Canonical Allele Identifier: PA916041642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 620612
ClinVar RCV Id: RCV000761072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2669Leu
CA16038597
NM_001354896.2:c.8005G>C