Canonical Allele Identifier: PA2826636183
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923264
ClinVar RCV Id: RCV001183837 RCV002298885 RCV003153936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val506Ile
CA346754013
NM_001281494.2:c.1516G>A