Canonical Allele Identifier: PA2825089135
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587334
ClinVar RCV Id: RCV003360812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu679Phe
CA346750735
NM_000179.3:c.2037G>C
CA346750736
NM_000179.3:c.2037G>T