Canonical Allele Identifier: PA286537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127279
ClinVar RCV Id: RCV000115071
ClinVar Variation Id: 628655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile638Leu
CA006331
NM_000038.6:c.1912A>T
CA16025497
NM_000038.6:c.1912A>C