Canonical Allele Identifier: PA2826463390
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573359
ClinVar RCV Id: RCV000695011 RCV002442461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser215Thr
CA346732821
NM_001258281.1:c.643T>A