Canonical Allele Identifier: PA348269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220313
ClinVar RCV Id: RCV000236701 RCV000568621 RCV003468948 RCV003997631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln2363His
CA047064
NM_001127511.3:c.7089A>C
CA16036888
NM_001127511.3:c.7089A>T