Canonical Allele Identifier: PA658804102
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525747
ClinVar RCV Id: RCV000630005 RCV001015381 RCV004002788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn798Thr
CA346730165
NM_000251.3:c.2393A>C