Canonical Allele Identifier: PA658689426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374
ClinVar RCV Id: RCV000587099 RCV001185311 RCV002530881 RCV003538394 RCV004002391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2656Gly
CA16038634
NM_001127510.3:c.7967A>G