Canonical Allele Identifier: PA2827990229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109
ClinVar RCV Id: RCV000236452 RCV000561345 RCV000779729 RCV002518420 RCV003535651 RCV003998895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2645Ala
CA049793
NM_001354900.2:c.7934T>C