Canonical Allele Identifier: PA2573164063
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356703
ClinVar RCV Id: RCV001880489 RCV002334744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala159Gly
CA346738596
NM_000179.3:c.476C>G