Canonical Allele Identifier: PA168762
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142587
ClinVar RCV Id: RCV000131790 RCV000588299 RCV000688511 RCV000855651 RCV003467187 RCV003998117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly287Ala
CA022444
NM_000251.3:c.860G>C