Canonical Allele Identifier: PA2827975921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388
ClinVar RCV Id: RCV000467558 RCV002451131 RCV002230486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1079Ser
CA16028614
NM_001354899.2:c.3235G>T