Canonical Allele Identifier: PA2827999471
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482515
ClinVar RCV Id: RCV000568183 RCV003767168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2681Ser
CA050195
NM_001354901.2:c.8041C>T