Canonical Allele Identifier: PA2826463684
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489908
ClinVar RCV Id: RCV000579738 RCV003886417 RCV003237947 RCV003758849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro283Ser
CA346733218
NM_001258281.1:c.847C>T