Canonical Allele Identifier: PA2828005790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411407
ClinVar RCV Id: RCV001013737 RCV003651856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser552Phe
CA16025529
NM_001354902.2:c.1655C>T