Canonical Allele Identifier: PA2826464131
Gene: MSH2 HGNC NCBI
ClinVar RCV:
RCV000076134
ClinVar Variation:
90638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met387Lys
CA018085
NM_001258281.1:c.1160T>A