Canonical Allele Identifier: PA2828017041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521
ClinVar RCV Id: RCV000034406 RCV000131447 RCV000210149 RCV000198399 RCV000254627 RCV000417343 RCV000677783 RCV003650358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala452Val
CA007259
NM_001354906.2:c.1355C>T