Canonical Allele Identifier: PA2827985048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1055767
ClinVar RCV Id: RCV003169834 RCV003771103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1079Arg
CA16028689
NM_001354900.2:c.3235G>A
CA16028690
NM_001354900.2:c.3235G>C