Canonical Allele Identifier: PA658831953
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619
ClinVar RCV Id: RCV000662519 RCV003650363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2622Leu
CA16038424
NM_001127510.3:c.7865C>T