Canonical Allele Identifier: PA2827972168
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_001341827.1:p.Asn2719Lys
CA16039202
NM_001354898.2:c.8157T>A
CA16039203
NM_001354898.2:c.8157T>G