Canonical Allele Identifier: PA164482
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141108
ClinVar RCV Id: RCV000129473 RCV000483264 RCV000779714 RCV002514719 RCV003650390 RCV003997504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala909Gly
CA007779
NM_001127511.3:c.2726C>G