Canonical Allele Identifier: PA645398783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236647
ClinVar RCV Id: RCV000229496 RCV000562662 RCV000677749 RCV001156936 RCV001193538 RCV003316239 RCV003477779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly253Ser
CA048563
NM_001127510.3:c.757G>A