Canonical Allele Identifier: PA297675
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181771
ClinVar RCV Id: RCV000159512 RCV000561698 RCV003474815 RCV003998394
ClinVar Variation Id: 1730863
ClinVar RCV Id: RCV002451872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu1129Phe
CA008358
NM_001127510.3:c.3387G>T
CA16028752
NM_001127510.3:c.3387G>C