Canonical Allele Identifier: PA2827986301
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490277
ClinVar RCV Id: RCV000581992 RCV003153754 RCV003653203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1455Ser
CA039198
NM_001354900.2:c.4364C>G
CA16031154
NM_001354900.2:c.4363A>T