Canonical Allele Identifier: PA2825089633
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791021
ClinVar RCV Id: RCV002450403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu807Asp
CA346754011
NM_000179.3:c.2421A>C
CA346754012
NM_000179.3:c.2421A>T