Canonical Allele Identifier: PA2827990700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146
ClinVar RCV Id: RCV000659278 RCV000570304 RCV003744539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2790Leu
CA050906
NM_001354900.2:c.8369C>T