Canonical Allele Identifier: PA2828012261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759033
ClinVar RCV Id: RCV002391439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2329Thr
CA16037571
NM_001354905.2:c.6985C>A