Canonical Allele Identifier: PA2827998072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232817
ClinVar RCV Id: RCV000215442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu2258Ser
CA046501
NM_001354901.2:c.6773T>C