Canonical Allele Identifier: PA645470936
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408509
ClinVar RCV Id: RCV000471952 RCV000574312 RCV004000785
ClinVar Variation Id: 573526
ClinVar RCV Id: RCV000695223 RCV002473115 RCV003460939 RCV003303146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser13Arg
CA16610974
NM_000251.3:c.39C>A
CA346728519
NM_000251.3:c.37A>C
CA346728528
NM_000251.3:c.39C>G