Canonical Allele Identifier: PA2827976955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met1385Val
CA009368
NM_001354899.2:c.4153A>G