Canonical Allele Identifier: PA2825644161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 971797
ClinVar RCV Id: RCV003652111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Phe2425Leu
CA16037285
NM_001127511.3:c.7273T>C
CA16037290
NM_001127511.3:c.7275C>A
CA16037291
NM_001127511.3:c.7275C>G