Canonical Allele Identifier: PA2827984706
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met973Val
CA16027984
NM_001354900.2:c.2917A>G