Canonical Allele Identifier: PA2826637808
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734598
ClinVar RCV Id: RCV002363816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu950Phe
CA346761092
NM_001281494.2:c.2850A>C
CA346761094
NM_001281494.2:c.2850A>T