Canonical Allele Identifier: PA2827980074
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met2336Leu
CA16036773
NM_001354899.2:c.7006A>C
CA16036774
NM_001354899.2:c.7006A>T