Canonical Allele Identifier: PA645398636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236580
ClinVar RCV Id: RCV000233150 RCV000491761 RCV000657055 RCV001818550 RCV002229774 RCV003743684 RCV003998663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu93Val
CA033407
NM_001127510.3:c.277C>G