Canonical Allele Identifier: PA349103
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219459
ClinVar RCV Id: RCV000204913 RCV000573936 RCV003997561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1081Asn
CA349100
NM_001127510.3:c.3242G>A