Canonical Allele Identifier: PA296816
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181340
ClinVar RCV Id: RCV000158791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr412Ser
CA010415
NM_000257.4:c.1234A>T
CA389051066
NM_000257.4:c.1235C>G