Canonical Allele Identifier: PA2827946929
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232817
ClinVar RCV Id: RCV000215442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Leu2317Ser
CA046501
NM_001354895.2:c.6950T>C