Canonical Allele Identifier: PA1139741894
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949059
ClinVar RCV Id: RCV003650741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2643Asn
CA16038441
NM_001354896.2:c.7928G>A