Canonical Allele Identifier: PA2827999238
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2613Val
CA16038743
NM_001354901.2:c.7838G>T