Canonical Allele Identifier: PA2826635559
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 998688
ClinVar RCV Id: RCV001294577 RCV002418882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met360Leu
CA346750631
NM_001281494.2:c.1078A>C
CA346750632
NM_001281494.2:c.1078A>T