Canonical Allele Identifier: PA286637
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127307
ClinVar RCV Id: RCV000115105 RCV000204622 RCV000575966 RCV000759434 RCV003997223 RCV003534340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1879Ser
CA010547
NM_000038.6:c.5635G>T