Canonical Allele Identifier: PA2826465272
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229972
ClinVar RCV Id: RCV000222756 RCV001361930 RCV001284504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met663Ile
CA020191
NM_001258281.1:c.1989G>T
CA10577999
NM_001258281.1:c.1989G>A
CA346729396
NM_001258281.1:c.1989G>C