Canonical Allele Identifier: PA2827970790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140854
ClinVar RCV Id: RCV000129062 RCV000480098 RCV002271411 RCV003325186 RCV003997477 RCV001824638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2301Gln
CA012730
NM_001354898.2:c.6902G>A