Canonical Allele Identifier: PA2828000667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780
ClinVar RCV Id: RCV000569755 RCV003537206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly546Arg
CA16025491
NM_001354902.2:c.1636G>A
CA16025492
NM_001354902.2:c.1636G>C