Canonical Allele Identifier: PA357269
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 218431
ClinVar RCV Id: RCV000219542 RCV000203004 RCV000410374 RCV000524152 RCV000774606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1034Trp
CA070044
NM_000179.3:c.3100C>T