Canonical Allele Identifier: PA2827990036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517
ClinVar RCV Id: RCV000034402 RCV000115124 RCV000254630 RCV000409244 RCV003534319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2589Ile
CA014160
NM_001354900.2:c.7765G>A