Canonical Allele Identifier: PA2826463275
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 630072
ClinVar RCV Id: RCV000774994 RCV000795234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn188Ser
CA346732382
NM_001258281.1:c.563A>G