Canonical Allele Identifier: PA916040390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231392
ClinVar RCV Id: RCV000215301 RCV002518304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1604Met
CA039747
NM_001354896.2:c.4811A>T