Canonical Allele Identifier: PA131072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41532
ClinVar RCV Id: RCV000034417 RCV000035077 RCV000167996 RCV000491791 RCV003315549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1798Asp
CA010373
NM_000038.6:c.5392A>G