Canonical Allele Identifier: PA645398877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234001
ClinVar RCV Id: RCV000219615 RCV001575306 RCV002516173 RCV003417795 RCV003650512 RCV003998591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro448Ala
CA027206
NM_001127510.3:c.1342C>G