Canonical Allele Identifier: PA2827966496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716842
ClinVar RCV Id: RCV003743862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1009Asp
CA16028128
NM_001354898.2:c.3027G>C
CA16028129
NM_001354898.2:c.3027G>T