Canonical Allele Identifier: PA658804042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537603
ClinVar RCV Id: RCV003538547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser52Gly
CA360612183
NM_001127511.3:c.154A>G