Canonical Allele Identifier: PA916039972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537524
ClinVar RCV Id: RCV001182318 RCV003153786 RCV003767865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu929Asp
CA033174
NM_001354896.2:c.2787A>T
CA16027291
NM_001354896.2:c.2787A>C