Canonical Allele Identifier: PA1139675057
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 921946
ClinVar RCV Id: RCV001181701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1583Ile
CA389037713
NM_000257.4:c.4749G>T
CA389037714
NM_000257.4:c.4749G>C
CA389037715
NM_000257.4:c.4749G>A