Canonical Allele Identifier: PA645402022
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640
ClinVar RCV Id: RCV000232680 RCV000236405 RCV000569669 RCV001705238 RCV003977640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly2370Val
CA046963
NM_001127510.3:c.7109G>T