Canonical Allele Identifier: PA2826635972
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 919663
ClinVar RCV Id: RCV001177975 RCV002265004 RCV003388603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu457Val
CA346752861
NM_001281494.2:c.1369C>G