Canonical Allele Identifier: PA2826626639
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230544
ClinVar RCV Id: RCV000223386 RCV000707381 RCV003997846
ClinVar Variation Id: 965508
ClinVar RCV Id: RCV001239977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val523Leu
CA068319
NM_001281492.2:c.1567G>C
CA46710015
NM_001281492.2:c.1567G>T