Canonical Allele Identifier: PA916040690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236620
ClinVar RCV Id: RCV000478919 RCV000561275 RCV001192984 RCV003535627 RCV003891805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1854Arg
CA042181
NM_001354896.2:c.5560G>A
CA16033377
NM_001354896.2:c.5560G>C