Canonical Allele Identifier: PA1139733901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469787
ClinVar RCV Id: RCV003392395 RCV003153715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val53Leu
CA124925269
NM_001354902.2:c.157G>C