Canonical Allele Identifier: PA645475569
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229770
ClinVar RCV Id: RCV000221755 RCV000464199 RCV000780438 RCV001843496 RCV002485413 RCV003997767 RCV004020644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr754Ser
CA035112
NM_000251.3:c.2260A>T
CA346729785
NM_000251.3:c.2261C>G