Canonical Allele Identifier: PA645398785
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236648
ClinVar RCV Id: RCV000574604 RCV001192799 RCV001699072 RCV003401163 RCV003535644 RCV003998691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His255Arg
CA048853
NM_001127510.3:c.764A>G