Canonical Allele Identifier: PA2827951601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141293
ClinVar RCV Id: RCV000129750 RCV000211911 RCV000412401 RCV001818303 RCV003315882 RCV003407543 RCV003997521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1293Thr
CA008695
NM_001354896.2:c.3878G>C