Canonical Allele Identifier: PA1139674991
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 922352
ClinVar RCV Id: RCV001182386 RCV003293938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1568Val
CA389037823
NM_000257.4:c.4702A>G