Canonical Allele Identifier: PA2826465054
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021808
ClinVar RCV Id: RCV001321629 RCV003150421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg614Leu
CA346729132
NM_001258281.1:c.1841G>T