Canonical Allele Identifier: PA645475229
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233888
ClinVar RCV Id: RCV000215510 RCV000462315 RCV000484436 RCV003454658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr677Arg
CA10577995
NM_000251.3:c.2030C>G