Canonical Allele Identifier: PA2827960168
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229993
ClinVar RCV Id: RCV000217420 RCV002494584 RCV003997790 RCV000237081 RCV003743647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg1886Met
CA042448
NM_001354897.2:c.5657G>T