Canonical Allele Identifier: PA2827961763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met2374Leu
CA16036773
NM_001354897.2:c.7120A>C
CA16036774
NM_001354897.2:c.7120A>T