Canonical Allele Identifier: PA2827991299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184601
ClinVar RCV Id: RCV000163884 RCV000411931 RCV001358755 RCV002228581 RCV003126560 RCV003995293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln164His
CA012417
NM_001354901.2:c.492A>C
CA16022798
NM_001354901.2:c.492A>T