Canonical Allele Identifier: PA2827978822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1018219
ClinVar RCV Id: RCV002543727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1953Lys
CA16034338
NM_001354899.2:c.5859T>A
CA16034339
NM_001354899.2:c.5859T>G