Canonical Allele Identifier: PA916040378
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393
ClinVar RCV Id: RCV000573193 RCV000806673 RCV001194205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1590Phe
CA039634
NM_001354896.2:c.4768A>T