Canonical Allele Identifier: PA645383379
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230117
ClinVar RCV Id: RCV000216842 RCV000227272 RCV000503628 RCV001080207 RCV003330587 RCV003997803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1027Leu
CA10578129
NM_000179.3:c.3079G>C
CA346756559
NM_000179.3:c.3079G>T