Canonical Allele Identifier: PA2825641662
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1616Leu
CA040139
NM_001127511.3:c.4847C>T