Canonical Allele Identifier: PA196946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187181
ClinVar RCV Id: RCV000166881 RCV003765043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2464Ala
CA013688
NM_001127511.3:c.7390C>G