Canonical Allele Identifier: PA1139741643
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 971797
ClinVar RCV Id: RCV003652111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Phe2461Leu
CA16037285
NM_001354896.2:c.7381T>C
CA16037290
NM_001354896.2:c.7383C>A
CA16037291
NM_001354896.2:c.7383C>G