Canonical Allele Identifier: PA2826636238
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 486894
ClinVar RCV Id: RCV000569376 RCV001853817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg518Ser
CA346754088
NM_001281494.2:c.1554G>C
CA346754089
NM_001281494.2:c.1554G>T