Canonical Allele Identifier: PA094647
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1764
ClinVar RCV Id: RCV000030245 RCV000130428 RCV000202220 RCV000376757 RCV000524366 RCV000763493 RCV001353396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala636Pro
CA019533
NM_000251.3:c.1906G>C