Canonical Allele Identifier: PA2827962826
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482372
ClinVar RCV Id: RCV000574631
ClinVar Variation Id: 936368
ClinVar RCV Id: RCV003650668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2692Leu
CA16038795
NM_001354897.2:c.8074G>C
CA16038796
NM_001354897.2:c.8074G>T