Canonical Allele Identifier: PA916041960
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566965
ClinVar RCV Id: RCV003534567
ClinVar Variation Id: 1770531
ClinVar RCV Id: RCV002387879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val460Leu
CA16024255
NM_001354897.2:c.1378G>C
CA16024256
NM_001354897.2:c.1378G>T