Canonical Allele Identifier: PA194125
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186196
ClinVar RCV Id: RCV000165743 RCV000529191 RCV003332132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu647Gln
CA019596
NM_000251.3:c.1939G>C