Canonical Allele Identifier: PA2826463315
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237407
ClinVar RCV Id: RCV000231079 RCV001026925 RCV001193895 RCV003128606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn197Lys
CA10582001
NM_001258281.1:c.591T>G
CA346732518
NM_001258281.1:c.591T>A