Canonical Allele Identifier: PA2826463795
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231153
ClinVar RCV Id: RCV000213803 RCV000483512 RCV001175089 RCV001080950 RCV001093680 RCV001355857 RCV003491975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln308Arg
CA027012
NM_001258281.1:c.923A>G