Canonical Allele Identifier: PA2826463078
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455601
ClinVar RCV Id: RCV000526049 RCV000579804 RCV001584241 RCV004003753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu139Gln
CA46678574
NM_001258281.1:c.415G>C