Canonical Allele Identifier: PA2828005782
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2830039
ClinVar RCV Id: RCV003744312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val551Leu
CA16025521
NM_001354902.2:c.1651G>C
CA16025522
NM_001354902.2:c.1651G>T