Canonical Allele Identifier: PA2826463740
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90541
ClinVar RCV Id: RCV000574719 RCV000629732 RCV003997140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn295Ser
CA017221
NM_001258281.1:c.884A>G