Canonical Allele Identifier: PA645400141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 245712
ClinVar RCV Id: RCV000491300 RCV000589170 RCV003650548 RCV003998900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1557Val
CA039538
NM_001127510.3:c.4669A>G