Canonical Allele Identifier: PA1139733313
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537655
ClinVar RCV Id: RCV003767868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro9Thr
CA360611647
NM_001354902.2:c.25C>A