Canonical Allele Identifier: PA2826465390
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307609
ClinVar RCV Id: RCV001763145 RCV004040161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly693Arg
CA346729809
NM_001258281.1:c.2077G>A
CA346729810
NM_001258281.1:c.2077G>C