Canonical Allele Identifier: PA2827999009
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 654022
ClinVar RCV Id: RCV003653372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu2544Asp
CA16038295
NM_001354901.2:c.7632A>C
CA16038296
NM_001354901.2:c.7632A>T