Canonical Allele Identifier: PA2827992038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566965
ClinVar RCV Id: RCV003534567
ClinVar Variation Id: 1770531
ClinVar RCV Id: RCV002387879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val391Leu
CA16024255
NM_001354901.2:c.1171G>C
CA16024256
NM_001354901.2:c.1171G>T