Canonical Allele Identifier: PA913194065
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 619263
ClinVar RCV Id: RCV000768485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile467Asn
CA389050705
NM_000257.4:c.1400T>A