Canonical Allele Identifier: PA2827949060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41505
ClinVar RCV Id: RCV000034387 RCV000122775 RCV000129715 RCV000211891 RCV000417265 RCV001155264 RCV003743546 RCV003944873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser130Gly
CA008731
NM_001354896.2:c.388A>G