Canonical Allele Identifier: PA2827977829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231258
ClinVar RCV Id: RCV000220997 RCV001775684 RCV003650484 RCV003997890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1653Leu
CA10578391
NM_001354899.2:c.4958C>T