Canonical Allele Identifier: PA297832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805
ClinVar RCV Id: RCV000159553 RCV000235095 RCV000210103 RCV000998414 RCV003534408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1358Val
CA008903
NM_001127510.3:c.4073C>T