Canonical Allele Identifier: PA2827963699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216017
ClinVar RCV Id: RCV000199388 RCV000501209 RCV001270008 RCV001853212
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg116Ser
CA338613
NM_001354898.2:c.348G>T
CA16022248
NM_001354898.2:c.348G>C