Canonical Allele Identifier: PA338141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216164
ClinVar RCV Id: RCV000198718 RCV000236990 RCV000446409 RCV000766728 RCV003534469 RCV003996975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1465Arg
CA038949
NM_001127510.3:c.4395T>A
CA16030951
NM_001127510.3:c.4393A>C
CA16030957
NM_001127510.3:c.4395T>G