Canonical Allele Identifier: PA645398872
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008
ClinVar RCV Id: RCV000590604 RCV001010961 RCV003470521 RCV003942584 RCV004002234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala440Thr
CA16024191
NM_001127510.3:c.1318G>A