Canonical Allele Identifier: PA2827986642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411531
ClinVar RCV Id: RCV000775710 RCV002230597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1554Ser
CA16031815
NM_001354900.2:c.4660G>T