Canonical Allele Identifier: PA2828000695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428139
ClinVar RCV Id: RCV000491162 RCV001357824 RCV002523967 RCV003535778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg562Gly
CA16025594
NM_001354902.2:c.1684A>G