Canonical Allele Identifier: PA2826463305
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185118
ClinVar RCV Id: RCV000164484 RCV002516464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met195Leu
CA022236
NM_001258281.1:c.583A>T
CA346732471
NM_001258281.1:c.583A>C