Canonical Allele Identifier: PA2825089166
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676789
ClinVar RCV Id: RCV003470245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe689Leu
CA346750785
NM_000179.3:c.2065T>C
CA346750790
NM_000179.3:c.2067C>A
CA346750791
NM_000179.3:c.2067C>G