Canonical Allele Identifier: PA2827971869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452710
ClinVar RCV Id: RCV003177484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu2630Val
CA16038627
NM_001354898.2:c.7889A>T