Canonical Allele Identifier: PA891846061
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 584612
ClinVar RCV Id: RCV000708854 RCV000809847 RCV002343578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala182Gly
CA346738735
NM_000179.3:c.545C>G