Canonical Allele Identifier: PA645399026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411357
ClinVar RCV Id: RCV000568317 RCV003651842 RCV002526440 RCV004001919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly857Arg
CA032593
NM_001127510.3:c.2569G>A
CA16026961
NM_001127510.3:c.2569G>C