Canonical Allele Identifier: PA645414661
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 431872
ClinVar RCV Id: RCV000497498 RCV000619314 RCV001857002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser180Thr
CA389052591
NM_000257.4:c.538T>A