Canonical Allele Identifier: PA2827971097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835
ClinVar RCV Id: RCV000478319 RCV000564092 RCV003535744 RCV002526526 RCV004002272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2396Leu
CA047405
NM_001354898.2:c.7187C>T