Canonical Allele Identifier: PA2826635542
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474116
ClinVar RCV Id: RCV001971032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val356Leu
CA346750606
NM_001281494.2:c.1066G>T
CA346750607
NM_001281494.2:c.1066G>C