Canonical Allele Identifier: PA2827989993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Phe2579Leu
CA16038407
NM_001354900.2:c.7735T>C
CA16038412
NM_001354900.2:c.7737T>A
CA16038413
NM_001354900.2:c.7737T>G