Canonical Allele Identifier: PA2827981360
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420277
ClinVar RCV Id: RCV000481602 RCV000567563 RCV002526568 RCV003493596 RCV003535753 RCV004003323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2721Thr
CA16039222
NM_001354899.2:c.8161T>A