Canonical Allele Identifier: PA2827954233
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1057153
ClinVar RCV Id: RCV003538750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro14Leu
CA360611732
NM_001354897.2:c.41C>T