Canonical Allele Identifier: PA658672732
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479829
ClinVar RCV Id: RCV000574655
ClinVar Variation Id: 491787
ClinVar RCV Id: RCV000584510 RCV000796750 RCV000735960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln601His
CA346728326
NM_000251.3:c.1803G>C
CA346728327
NM_000251.3:c.1803G>T