Canonical Allele Identifier: PA2827959502
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1501504
ClinVar RCV Id: RCV003773324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg1686Ser
CA16032329
NM_001354897.2:c.5058A>C
CA16032330
NM_001354897.2:c.5058A>T