Canonical Allele Identifier: PA645401978
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232817
ClinVar RCV Id: RCV000215442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2317Ser
CA046501
NM_001127510.3:c.6950T>C