Canonical Allele Identifier: PA2825091975
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 653382
ClinVar RCV Id: RCV000809152
ClinVar Variation Id: 940856
ClinVar RCV Id: RCV001210530 RCV002460136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1212Leu
CA346760609
NM_000179.3:c.3634G>C
CA346760610
NM_000179.3:c.3634G>T