Canonical Allele Identifier: PA2827956952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar RCV Id: RCV000216931 RCV000235531 RCV003765426 RCV003997973
ClinVar Variation Id: 663857
ClinVar RCV Id: RCV001016394 RCV004002836 RCV003537293 RCV003141857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly917Arg
CA033124
NM_001354897.2:c.2749G>A
CA033134
NM_001354897.2:c.2749G>C