Canonical Allele Identifier: PA094901
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90878
ClinVar RCV Id: RCV000076380 RCV000491588 RCV000821619
ClinVar Variation Id: 428477
ClinVar RCV Id: RCV000490901 RCV001378609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly692Arg
CA019963
NM_000251.3:c.2074G>C
CA346729188
NM_000251.3:c.2074G>A