Canonical Allele Identifier: PA357486
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220143
ClinVar RCV Id: RCV000204923 RCV000485879 RCV000657010 RCV001026289 RCV001142203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile245Leu
CA073402
NM_000179.3:c.733A>T
CA346740047
NM_000179.3:c.733A>C