Canonical Allele Identifier: PA2827983268
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1041944
ClinVar RCV Id: RCV003770958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu507Phe
CA16024899
NM_001354900.2:c.1521G>C
CA16024900
NM_001354900.2:c.1521G>T