Canonical Allele Identifier: PA2826465732
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141042
ClinVar RCV Id: RCV000129378 RCV000410280 RCV000480490 RCV000532767 RCV000767208 RCV003997498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu786Asp
CA020728
NM_001258281.1:c.2358G>C
CA346730899
NM_001258281.1:c.2358G>T