Canonical Allele Identifier: PA916042139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571507
ClinVar RCV Id: RCV000777314 RCV002532218
ClinVar Variation Id: 3230828
ClinVar RCV Id: RCV004522942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met210Ile
CA16022647
NM_001354902.2:c.630G>A
CA16022648
NM_001354902.2:c.630G>C
CA16022649
NM_001354902.2:c.630G>T