Canonical Allele Identifier: PA2827970869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887
ClinVar RCV Id: RCV000507925 RCV002524428 RCV003159638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2327Asn
CA16036703
NM_001354898.2:c.6980G>A