Canonical Allele Identifier: PA2830458305
Gene: KRTAP10-8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3116896
ClinVar RCV Id: RCV004414744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_941968.2:p.Leu72Val
CA410476984
NM_198695.2:c.214C>G