Canonical Allele Identifier: PA2827940699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1720103
ClinVar RCV Id: RCV003743904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg399Ser
CA16023926
NM_001354895.2:c.1197A>C
CA16023927
NM_001354895.2:c.1197A>T