Canonical Allele Identifier: PA2828019048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167
ClinVar RCV Id: RCV000491915 RCV000502196 RCV001353697 RCV003148754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn925Thr
CA16028070
NM_001354903.2:c.2774A>C