Canonical Allele Identifier: PA915984283
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216361
ClinVar RCV Id: RCV000197496 RCV000579889 RCV000780448 RCV000662894 RCV001569704 RCV001798671 RCV003997024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly91Ala
CA038898
NM_001258281.1:c.272G>C