Canonical Allele Identifier: PA916041905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 217920
ClinVar RCV Id: RCV000202029 RCV000466853 RCV000571880 RCV000657057 RCV003534474 RCV003997040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala425Thr
CA026910
NM_001354897.2:c.1273G>A