Canonical Allele Identifier: PA916011861
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455253
ClinVar RCV Id: RCV000525940 RCV000579610 RCV004003691 RCV003225079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val830Leu
CA070770
NM_001281494.2:c.2488G>C