Canonical Allele Identifier: PA2827971297
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_001341827.1:p.Pro2457Ala
CA013688
NM_001354898.2:c.7369C>G