Allele Registry

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Canonical Allele Identifier: PA2826464783

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447487

ClinVar RCV Id: RCV001996806

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly548Arg	CA346728394 NM_001258281.1:c.1642G>A CA346728395 NM_001258281.1:c.1642G>C