Canonical Allele Identifier: PA645473504
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419016
ClinVar RCV Id: RCV000479898 RCV000561329 RCV000629790 RCV001821392 RCV004002282
ClinVar Variation Id: 3069732
ClinVar RCV Id: RCV004009764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val363Leu
CA026946
NM_000251.3:c.1087G>T
CA346733541
NM_000251.3:c.1087G>C