Canonical Allele Identifier: PA2827987122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466
ClinVar RCV Id: RCV000580755 RCV003767263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1701Leu
CA16032754
NM_001354900.2:c.5102G>T