Canonical Allele Identifier: PA2827966742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420874
ClinVar RCV Id: RCV000478947 RCV001019909 RCV003493598 RCV003470563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg1080Trp
CA034994
NM_001354898.2:c.3238C>T