Canonical Allele Identifier: PA2826465213
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820732
ClinVar RCV Id: RCV001014475 RCV001860762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly647Glu
CA034328
NM_001258281.1:c.1940G>A