Canonical Allele Identifier: PA2825644813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761367
ClinVar RCV Id: RCV002416871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2634Tyr
CA16038605
NM_001127511.3:c.7901C>A