Canonical Allele Identifier: PA2826462756
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237389
ClinVar RCV Id: RCV000229561 RCV000235910 RCV000491448 RCV003150133 RCV003998761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val12Ile
CA035416
NM_001258281.1:c.34G>A