Canonical Allele Identifier: PA2825092961
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1737222
ClinVar RCV Id: RCV002321180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1345Leu
CA346761680
NM_000179.3:c.4033G>C
CA346761681
NM_000179.3:c.4033G>T