Canonical Allele Identifier: PA1139741850
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 918607
ClinVar RCV Id: RCV001176273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2594Pro
CA16038109
NM_001354896.2:c.7780G>C