Canonical Allele Identifier: PA645402269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411449
ClinVar RCV Id: RCV000567469 RCV003766578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2531Ala
CA16037824
NM_001127510.3:c.7591T>G