Canonical Allele Identifier: PA2826463841
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90556
ClinVar RCV Id: RCV000794953 RCV001010013 RCV001538801 RCV003997142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro319Leu
CA017372
NM_001258281.1:c.956C>T