Canonical Allele Identifier: PA645417243
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 423269
ClinVar RCV Id: RCV000481324 RCV003748231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1561Pro
CA16619846
NM_000257.4:c.4681G>C