Canonical Allele Identifier: PA2827966468
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_001341827.1:p.Asn1001Thr
CA16028070
NM_001354898.2:c.3002A>C