Canonical Allele Identifier: PA891844991
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 583204
ClinVar RCV Id: RCV000707479 RCV001186494 RCV002343575 RCV001766567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1671Val
CA389037138
NM_000257.4:c.5011A>G