Canonical Allele Identifier: PA916040567
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184596
ClinVar RCV Id: RCV000163875 RCV000205541 RCV000589784 RCV003995292 RCV003233477 RCV003316011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1757Arg
CA009933
NM_001354896.2:c.5270A>G