Canonical Allele Identifier: PA331614
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91119
ClinVar RCV Id: RCV000570883 RCV000627693 RCV001137124 RCV003231115 RCV003997176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg171Lys
CA021254
NM_000251.3:c.512G>A