Canonical Allele Identifier: PA2825640097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490262
ClinVar RCV Id: RCV000581738 RCV003153753 RCV004001289 RCV003767285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Tyr1117Cys
CA035239
NM_001127511.3:c.3350A>G