Canonical Allele Identifier: PA098613
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14097
ClinVar RCV Id: RCV000015153 RCV000035820 RCV000078452 RCV000247943 RCV000458449 RCV001177579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu908Val
CA012953
NM_000257.4:c.2722C>G