Canonical Allele Identifier: PA2827964515
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2848588
ClinVar RCV Id: RCV003744521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp371Glu
CA16023905
NM_001354898.2:c.1113T>A
CA16023906
NM_001354898.2:c.1113T>G