Canonical Allele Identifier: PA2827956110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2681902
ClinVar RCV Id: RCV003477194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly645Arg
CA16025480
NM_001354897.2:c.1933G>A
CA16025481
NM_001354897.2:c.1933G>C