Canonical Allele Identifier: PA098880
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14113
ClinVar RCV Id: RCV000015169 RCV000819604 RCV002408466 RCV003319167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser642Leu
CA011471
NM_000257.4:c.1925C>T