Canonical Allele Identifier: PA913192468
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628496
ClinVar RCV Id: RCV000772969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser677Arg
CA346750717
NM_000179.3:c.2029A>C
CA346750722
NM_000179.3:c.2031T>G
CA346750723
NM_000179.3:c.2031T>A