Canonical Allele Identifier: PA2827957339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1038Ile
CA16028086
NM_001354897.2:c.3113G>T