Canonical Allele Identifier: PA2827969579
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127309
ClinVar RCV Id: RCV000115107 RCV000232068 RCV000491906 RCV001255490 RCV003534341
ClinVar Variation Id: 141168
ClinVar RCV Id: RCV000129560 RCV000411270 RCV000985310 RCV001155576 RCV003315876 RCV003997510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1935Leu
CA010751
NM_001354898.2:c.5804_5805delinsTA
CA010760
NM_001354898.2:c.5804C>T