Canonical Allele Identifier: PA2828041766
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_001341833.1:p.Met1512Ile
CA16032097
NM_001354904.2:c.4536G>A
CA16032098
NM_001354904.2:c.4536G>C
CA16032099
NM_001354904.2:c.4536G>T