Canonical Allele Identifier: PA2573165150
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1481330
ClinVar RCV Id: RCV001994154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1363Asn
CA389040969
NM_000257.4:c.4089G>T
CA389040971
NM_000257.4:c.4089G>C