Canonical Allele Identifier: PA296750
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181300
ClinVar RCV Id: RCV000158728 RCV000543876 RCV000825644 RCV001524837 RCV002453549 RCV002492628
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile114Thr
CA013685
NM_000257.4:c.341T>C