Canonical Allele Identifier: PA2825644907
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482372
ClinVar RCV Id: RCV000574631
ClinVar Variation Id: 936368
ClinVar RCV Id: RCV003650668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val2664Leu
CA16038795
NM_001127511.3:c.7990G>C
CA16038796
NM_001127511.3:c.7990G>T