Canonical Allele Identifier: PA916040539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629228
ClinVar RCV Id: RCV000773927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1739Val
CA16032616
NM_001354896.2:c.5216G>T