Canonical Allele Identifier: PA916040786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472
ClinVar RCV Id: RCV001024497 RCV003651873 RCV002523386 RCV004001955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1939Ser
CA16033936
NM_001354896.2:c.5815G>A