Canonical Allele Identifier: PA658680261
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455341
ClinVar RCV Id: RCV000526816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly237Arg
CA346739987
NM_000179.3:c.709G>A
CA346739988
NM_000179.3:c.709G>C