Canonical Allele Identifier: PA2826634781
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188121
ClinVar RCV Id: RCV000579821 RCV001317757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val181Leu
CA008628
NM_001281494.2:c.541G>C
CA346745676
NM_001281494.2:c.541G>T