Canonical Allele Identifier: PA2828002736
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1421607
ClinVar RCV Id: RCV002558421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1604Thr
CA16032445
NM_001354902.2:c.4811G>C