Canonical Allele Identifier: PA916042000
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser987Ile
CA16028086
NM_001354900.2:c.2960G>T