Canonical Allele Identifier: PA296506
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181163
ClinVar RCV Id: RCV000158495 RCV000416097 RCV001201625 RCV003998353
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1399Asp
CA014617
NM_000257.4:c.4197A>T
CA389040539
NM_000257.4:c.4197A>C