Canonical Allele Identifier: PA2826465482
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185569
ClinVar RCV Id: RCV000165012 RCV000196615 RCV000522265 RCV000587565 RCV003462160 RCV003995381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His719Pro
CA020494
NM_001258281.1:c.2156A>C