Canonical Allele Identifier: PA2827971639
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1476541
ClinVar RCV Id: RCV003773114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys2560Arg
CA16038172
NM_001354898.2:c.7679A>G