Canonical Allele Identifier: PA2579910154
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071026
ClinVar RCV Id: RCV004014528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu86Asp
CA346729547
NM_000251.3:c.258A>T
CA346729548
NM_000251.3:c.258A>C