Canonical Allele Identifier: PA2827956886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135694
ClinVar RCV Id: RCV000122768 RCV000485846 RCV000664308 RCV000574171 RCV001157044 RCV003315799 RCV003997374 RCV003325185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln896His
CA007712
NM_001354897.2:c.2688G>T
CA16027135
NM_001354897.2:c.2688G>C