Canonical Allele Identifier: PA098917
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42992
ClinVar RCV Id: RCV000208315 RCV000518840 RCV000552931 RCV000617360 RCV001171198 RCV001807755 RCV002504879 RCV004528172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1377Met
CA014494
NM_000257.4:c.4130C>T