Canonical Allele Identifier: PA645398941
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954
ClinVar RCV Id: RCV000222920 RCV003335256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser634Arg
CA10578330
NM_001127510.3:c.1902T>G
CA16025473
NM_001127510.3:c.1900A>C
CA16025479
NM_001127510.3:c.1902T>A