Canonical Allele Identifier: PA2826464173
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419371
ClinVar RCV Id: RCV000478449 RCV000572368 RCV001210873 RCV004002297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val397Met
CA16617578
NM_001258281.1:c.1189G>A