Canonical Allele Identifier: PA916010969
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140779
ClinVar RCV Id: RCV000128922 RCV000220784 RCV000226897 RCV000412094 RCV000780475 RCV001356921 RCV003153411 RCV003149883 RCV003323293 RCV004532539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala36Val
CA007963
NM_001281492.2:c.107C>T