Canonical Allele Identifier: PA2827959392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1172116
ClinVar RCV Id: RCV001525745 RCV003653479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met1648Ile
CA16032097
NM_001354897.2:c.4944G>A
CA16032098
NM_001354897.2:c.4944G>C
CA16032099
NM_001354897.2:c.4944G>T