Canonical Allele Identifier: PA338617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216017
ClinVar RCV Id: RCV000199388 RCV000501209 RCV001270008 RCV001853212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg141Ser
CA338613
NM_001127510.3:c.423G>T
CA16022248
NM_001127510.3:c.423G>C