Canonical Allele Identifier: PA2828004135
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567031
ClinVar RCV Id: RCV003278300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile2424Leu
CA16037724
NM_001354902.2:c.7270A>C
CA16037725
NM_001354902.2:c.7270A>T