Canonical Allele Identifier: PA2826625262
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823498
ClinVar RCV Id: RCV001019792 RCV001860958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser198Gly
CA346741038
NM_001281492.2:c.592A>G