Canonical Allele Identifier: PA915957393
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 647534
ClinVar RCV Id: RCV000802060 RCV001185407 RCV002325544 RCV002501075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1366Leu
CA040392
NM_000257.4:c.4097C>T