Canonical Allele Identifier: PA2827971319
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487042
ClinVar RCV Id: RCV000574906 RCV001755962 RCV003767245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2465Gly
CA16037580
NM_001354898.2:c.7394A>G