Canonical Allele Identifier: PA189696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536
ClinVar RCV Id: RCV000034421 RCV000122803 RCV000148373 RCV000163980 RCV000236063 RCV003650359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile2555Val
CA013990
NM_001127511.3:c.7663A>G