Canonical Allele Identifier: PA299535
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89362
ClinVar RCV Id: RCV000074829 RCV000160725 RCV000524164 RCV000586012 RCV000764430 RCV003149721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1087Arg
CA012273
NM_000179.3:c.3260C>G