Canonical Allele Identifier: PA645385148
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233214
ClinVar RCV Id: RCV000219938 RCV000459481 RCV001810439 RCV003316228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1334Pro
CA10578173
NM_000179.3:c.4001G>C