Canonical Allele Identifier: PA658660356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050
ClinVar RCV Id: RCV002358548 RCV003470762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2170Ser
CA16035571
NM_001127510.3:c.6508C>T