Canonical Allele Identifier: PA2827989112
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82634
ClinVar RCV Id: RCV000073623 RCV001180823 RCV003153342 RCV003534326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2309Tyr
CA012776
NM_001354900.2:c.6926C>A