Canonical Allele Identifier: PA2573062019
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333012
ClinVar RCV Id: RCV001807701 RCV002274211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1560Pro
CA389037873
NM_000257.4:c.4679G>C