Canonical Allele Identifier: PA915984008
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483749
ClinVar RCV Id: RCV000567001 RCV000793779 RCV004001043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg40Thr
CA346729684
NM_001258281.1:c.119G>C