Canonical Allele Identifier: PA2826462999
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483679
ClinVar RCV Id: RCV000574683 RCV000810913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu121Phe
CA346730909
NM_001258281.1:c.361C>T