Canonical Allele Identifier: PA2827990319
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2672Val
CA16039002
NM_001354900.2:c.8014A>G