Canonical Allele Identifier: PA2825629640
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met1014Val
CA16027984
NM_001127510.3:c.3040A>G