Canonical Allele Identifier: PA2827990012
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489499
ClinVar RCV Id: RCV000579961 RCV003153750 RCV003537237 RCV004001235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2583Asp
CA16038432
NM_001354900.2:c.7747A>G