Canonical Allele Identifier: PA2827977419
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452682
ClinVar RCV Id: RCV003177456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln1521His
CA16031514
NM_001354899.2:c.4563A>C
CA16031515
NM_001354899.2:c.4563A>T