Canonical Allele Identifier: PA195658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186722
ClinVar RCV Id: RCV000166364 RCV000473143 RCV000482783 RCV002478515 RCV003995502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu2493Phe
CA013771
NM_001127511.3:c.7477C>T