Canonical Allele Identifier: PA2826635672
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410509
ClinVar RCV Id: RCV000460149 RCV000775722 RCV001576673 RCV001797726 RCV004001851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly384Cys
CA16610900
NM_001281494.2:c.1150G>T