Canonical Allele Identifier: PA2499230360
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1075461
ClinVar RCV Id: RCV001389062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1597Pro
CA389037628
NM_000257.4:c.4790T>C