Canonical Allele Identifier: PA330623
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89564
ClinVar RCV Id: RCV000215096 RCV000220612 RCV000630227 RCV000662409 RCV003460703 RCV003997102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile251Val
CA016421
NM_000179.3:c.751A>G