Canonical Allele Identifier: PA2826463197
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127651
ClinVar RCV Id: RCV000115540 RCV000543104 RCV000567353 RCV003997282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile171Val
CA022070
NM_001258281.1:c.511A>G