Canonical Allele Identifier: PA2827957669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127287
ClinVar RCV Id: RCV000115081 RCV000569678 RCV001251414 RCV003997214 RCV003650369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln1133Pro
CA008326
NM_001354897.2:c.3398A>C