Canonical Allele Identifier: PA2827980799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489496
ClinVar RCV Id: RCV000580381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2553Thr
CA16038144
NM_001354899.2:c.7658G>C