Canonical Allele Identifier: PA2827954385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val53Leu
CA124925269
NM_001354897.2:c.157G>C