Canonical Allele Identifier: PA645400207
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411445
ClinVar RCV Id: RCV000572779 RCV000483622 RCV003766576 RCV004001948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1695Gly
CA040621
NM_001127510.3:c.5083A>G