Canonical Allele Identifier: PA2828040995
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_001341833.1:p.Gln1423His
CA16031514
NM_001354904.2:c.4269A>C
CA16031515
NM_001354904.2:c.4269A>T