Canonical Allele Identifier: PA1139671808
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 849519
ClinVar RCV Id: RCV001053505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr255Lys
CA389052102
NM_000257.4:c.764C>A