Canonical Allele Identifier: PA2573164060
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482192
ClinVar RCV Id: RCV002025111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg146Ser
CA346737173
NM_000179.3:c.438G>C
CA346737174
NM_000179.3:c.438G>T