Canonical Allele Identifier: PA2827991861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700
ClinVar RCV Id: RCV001174750 RCV000572587 RCV003999359 RCV003535809 RCV002491068 RCV003322784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys339Arg
CA026866
NM_001354901.2:c.1016A>G