Canonical Allele Identifier: PA2827994759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1252Ser
CA10578361
NM_001354901.2:c.3755T>G