Canonical Allele Identifier: PA297765
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181791
ClinVar RCV Id: RCV000159537 RCV000491278 RCV000766428 RCV001353861 RCV003998407 RCV003534402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly635Ala
CA006287
NM_001127510.3:c.1904G>C