Canonical Allele Identifier: PA2826463566
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91260
ClinVar RCV Id: RCV000148634 RCV000222150 RCV000412467 RCV000480555 RCV000524426 RCV003997184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser257Cys
CA022662
NM_001258281.1:c.770C>G