Canonical Allele Identifier: PA2828030093
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2827950
ClinVar RCV Id: RCV003744279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2461Lys
CA16039202
NM_001354906.2:c.7383T>A
CA16039203
NM_001354906.2:c.7383T>G