Canonical Allele Identifier: PA2827974168
Gene: APC HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu520Phe
CA16024899
NM_001354899.2:c.1560G>C
CA16024900
NM_001354899.2:c.1560G>T