Canonical Allele Identifier: PA916042494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41502
ClinVar RCV Id: RCV000034384 RCV000077988 RCV000115083 RCV000196915 RCV000203169 RCV000393833 RCV001353808 RCV003996152 RCV003534314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Leu969Ser
CA008351
NM_001354905.2:c.2906T>C