Canonical Allele Identifier: PA349849
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743
ClinVar RCV Id: RCV000236966 RCV000571447 RCV001264579 RCV003743632 RCV003967554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1108Ser
CA035035
NM_001127510.3:c.3323A>G