Canonical Allele Identifier: PA2828023013
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_001341835.1:p.Arg1393Ser
CA16032329
NM_001354906.2:c.4179A>C
CA16032330
NM_001354906.2:c.4179A>T