Canonical Allele Identifier: PA916041467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522
ClinVar RCV Id: RCV000120032 RCV000131590 RCV000587624 RCV001153055 RCV003323291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2515Leu
CA013717
NM_001354896.2:c.7544C>T