Canonical Allele Identifier: PA163613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705
ClinVar RCV Id: RCV000122783 RCV000128987 RCV000236885 RCV000586353 RCV003534357 RCV001353632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1652Val
CA009818
NM_001127511.3:c.4955C>T